Facet engineering of oxide nanocrystals represents a powerful method for generating diverse properties for practical and innovative applications. Therefore, it is crucial to determine the nature of the exposed facets of oxides in order to develop the facet/morphology–property relationships and rationally design nanostructures with desired properties. Despite the extensive applications of electron microscopy for visualizing the facet structure of nanocrystals, the volumes sampled by such techniques are very small and may not be representative of the whole sample. Here, we develop a convenient 17O nuclear magnetic resonance (NMR) strategy to distinguish oxide nanocrystals exposing different facets. In combination with density functional theory calculations, we show that the oxygen ions on the exposed (001) and (101) facets of anatase titania nanocrystals have distinct 17O NMR shifts, which are sensitive to surface reconstruction and the nature of the steps on the surface. The results presented here open up methods for characterizing faceted nanocrystalline oxides and related materials.
S = 1 /2 kagome lattice antiferromagnets (KLAFs) have attracted great interest since they are closely associated with the long-sought quantum spin liquid (QSL) state. The realization of S = 1/2 KLAF remains an outstanding challenge and efforts have focused principally on Cu2+, d9 compounds. Herein, the synthesis of the first structurally perfect d1 KLAF, (CH3NH3)2NaTi3F12, is presented. The trivalent oxidation state and the Jahn-Teller distortion of Ti3+ ions are probed by single crystal X-ray diffraction, X-ray photoelectron spectroscopy, and UV-vis-NIR diffuse reflectance. No structural phase transitions can be observed from 1.8 K to 523 K. However, a glass transition can be observed due to the disordered, interlayer CH3NH3+ cations.The Curie-Weiss temperature, θcw= -139.5(7) K, and the lack of long-range ordering in magnetic susceptibility and specific heat imply that this compound is a QSL candidate.
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The
recent isolation of molecular tetravalent lanthanide complexes
has enabled renewed exploration of the effect of oxidation state on
the single-ion properties of the lanthanide ions. Despite the isotropic
nature of the 8S ground state in a tetravalent terbium
complex, [Tb(NP(1,2-bis-
t
Bu-diamidoethane)(NEt2))4], preliminary X-band electron paramagnetic
resonance (EPR) measurements on tetravalent terbium complexes show
rich spectra with broad resonances. The complexity of these spectra
highlights the limits of conventional X-band EPR for even qualitative
determination of zero-field splitting (ZFS) in these complexes. Therefore,
we report the synthesis and characterization of a novel valence series
of 4f7 molecular complexes spanning three oxidation states
(Eu2+, Gd3+, and Tb4+) featuring
a weak-field imidophosphorane ligand system, and employ high-frequency
and -field electron paramagnetic resonance (HFEPR) to obtain quantitative
values for ZFS across this valence series. The series was designed
to minimize deviation in the first coordination sphere from the pseudotetrahedral
geometry in order to directly interrogate the role of metal identity
and charge on the complexes’ electronic structures. These HFEPR
studies are supported by crystallographic analysis and quantum-chemical
calculations to assess the relative covalent interactions in each
member of this valence series and the effect of the oxidation state
on the splitting of the ground state and first excited state.
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